Literature DB >> 18027208

Innovative approaches for designing and analyzing adaptive dose-ranging trials.

Björn Bornkamp1, Frank Bretz, Alex Dmitrienko, Greg Enas, Brenda Gaydos, Chyi-Hung Hsu, Franz König, Michael Krams, Qing Liu, Beat Neuenschwander, Tom Parke, José Pinheiro, Amit Roy, Rick Sax, Frank Shen.   

Abstract

Inadequate selection of the dose to bring forward in confirmatory trials has been identified as one of the key drivers of the decreasing success rates observed in drug development programs across the pharmaceutical industry. In recognition of this problem, the Pharmaceutical Research and Manufacturers of America (PhRMA), formed a working group to evaluate and develop alternative approaches to dose finding, including adaptive dose-ranging designs. This paper summarizes the work of the group, including the results and conclusions of a comprehensive simulation study, and puts forward recommendations on how to improve dose ranging in clinical development, including, but not limited to, the use of adaptive dose-ranging methods.

Mesh:

Year:  2007        PMID: 18027208     DOI: 10.1080/10543400701643848

Source DB:  PubMed          Journal:  J Biopharm Stat        ISSN: 1054-3406            Impact factor:   1.051


  30 in total

1.  Adaptive optimal design for bridging studies with an application to population pharmacokinetic studies.

Authors:  Lee Kien Foo; Stephen Duffull
Journal:  Pharm Res       Date:  2012-02-14       Impact factor: 4.200

2.  An example of optimal phase II design for exposure response modelling.

Authors:  Alan Maloney; Marloes Schaddelee; Jan Freijer; Walter Krauwinkel; Marcel van Gelderen; Philippe Jacqmin; Ulrika S H Simonsson
Journal:  J Pharmacokinet Pharmacodyn       Date:  2010-09-25       Impact factor: 2.745

Review 3.  The future of drug development: advancing clinical trial design.

Authors:  John Orloff; Frank Douglas; Jose Pinheiro; Susan Levinson; Michael Branson; Pravin Chaturvedi; Ene Ette; Paul Gallo; Gigi Hirsch; Cyrus Mehta; Nitin Patel; Sameer Sabir; Stacy Springs; Donald Stanski; Matthias R Evers; Edd Fleming; Navjot Singh; Tony Tramontin; Howard Golub
Journal:  Nat Rev Drug Discov       Date:  2009-10-09       Impact factor: 84.694

4.  An overview of the adaptive designs accelerating promising trials into treatments (ADAPT-IT) project.

Authors:  William J Meurer; Roger J Lewis; Danilo Tagle; Michael D Fetters; Laurie Legocki; Scott Berry; Jason Connor; Valerie Durkalski; Jordan Elm; Wenle Zhao; Shirley Frederiksen; Robert Silbergleit; Yuko Palesch; Donald A Berry; William G Barsan
Journal:  Ann Emerg Med       Date:  2012-03-15       Impact factor: 5.721

5.  Practical considerations for optimal designs in clinical dose finding studies.

Authors:  Frank Bretz; Holger Dette; Jose C Pinheiro
Journal:  Stat Med       Date:  2010-03-30       Impact factor: 2.373

6.  Comparison of Model Averaging and Model Selection in Dose Finding Trials Analyzed by Nonlinear Mixed Effect Models.

Authors:  Simon Buatois; Sebastian Ueckert; Nicolas Frey; Sylvie Retout; France Mentré
Journal:  AAPS J       Date:  2018-03-29       Impact factor: 4.009

7.  Feasibility of Exposure-Response Analyses for Clinical Dose-Ranging Studies of Drug Combinations.

Authors:  Theodoros Papathanasiou; Anders Strathe; Andrew C Hooker; Trine Meldgaard Lund; Rune Viig Overgaard
Journal:  AAPS J       Date:  2018-04-23       Impact factor: 4.009

8.  An adaptive two-stage dose-response design method for establishing proof of concept.

Authors:  Yoko Franchetti; Stewart J Anderson; Allan R Sampson
Journal:  J Biopharm Stat       Date:  2013       Impact factor: 1.051

9.  Overview, hurdles, and future work in adaptive designs: perspectives from a National Institutes of Health-funded workshop.

Authors:  Christopher S Coffey; Bruce Levin; Christina Clark; Cate Timmerman; Janet Wittes; Peter Gilbert; Sara Harris
Journal:  Clin Trials       Date:  2012-12       Impact factor: 2.486

10.  Good Practices in Model-Informed Drug Discovery and Development: Practice, Application, and Documentation.

Authors:  S F Marshall; R Burghaus; V Cosson; S Y A Cheung; M Chenel; O DellaPasqua; N Frey; B Hamrén; L Harnisch; F Ivanow; T Kerbusch; J Lippert; P A Milligan; S Rohou; A Staab; J L Steimer; C Tornøe; S A G Visser
Journal:  CPT Pharmacometrics Syst Pharmacol       Date:  2016-03-14
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